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Objective Classification of Neocortical Pyramidal Cells

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Objective Classification of Neocortical Pyramidal Cells bioRxiv preprint doi: https://doi.org/10.1101/349977; this version posted June 19, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Objective Classification of Neocortical Pyramidal Cells Lida Kanari1*, Srikanth Ramaswamy1*, Ying Shi1*, Sebastien Morand2, Julie Meystre3, Rodrigo Perin3, Marwan Abdellah1, Yun Wang4,5+, Kathryn Hess2+, and Henry Markram1,3+ 1Blue Brain Project, Brain & Mind Institute, EPFL, Geneva, Switzerland. 2Laboratory for Topology and Neuroscience, Brain Mind Institute, EPFL, Lausanne, Switzerland 3Laboratory of Neural Microcircuitry, Brain Mind Institute, EPFL, Lausanne, Switzerland; 4School of Optometry & Ophthalmology, Wenzhou Medical College, Wenzhou, Zhejiang, P.R.China; 5Allen Institute for Brain Science, Seattle, WA, USA; *Co-first authors +Senior authors Correspondance: lida.k anar [email protected] [email protected] bioRxiv preprint doi: https://doi.org/10.1101/349977; this version posted June 19, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Abstract A consensus on the number of morphologically different types of pyramidal cells (PCs) in the neocortex has not yet been reached, despite over a century of anatomical studies. This is because of a lack of agreement on the subjective classifications of neuron types, which is based on expert analyses of neuronal morphologies: the shapes of somata, dendrites, and axons. Even for neurons that are visually different to non-experts, there is no common ground to consistently distinguish morphological types. We found that objective classification is possible with methods from algebraic topology, and that the dendritic arbor is sufficient for reliable identification of distinct types of PCs. We also provide a solution for the more challenging problem of whether two similar neurons belong to different types or to a continuum of the same type. Using this scheme, we objectively identify seventeen types of PCs in the rat somatosensory cortex. Our topological classification does not require expert input, is stable, and helps settle the long-standing debate on whether cell-types are discrete or continuous morphological variations of each other. Key words Rat Somatosensory Cortex, Pyramidal Cells, Neuronal Morphology, Topological Data Analysis, Neuronal Classification bioRxiv preprint doi: https://doi.org/10.1101/349977; this version posted June 19, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Introduction The mammalian neocortex is comprised of about 85% excitatory pyramidal cells (PCs), and around 15% inhibitory interneurons (Ramón y Cajal 1911; DeFelipe and Farinas 1992; Spruston 2007; Markram et al. 2015; Ramaswamy and Markram 2015). PCs, also termed principal cells, are characterized by a triangular soma, two distinct dendritic domains, both of which exhibit a high density of spines, emanating from the base (basal dendrites) and the apex of the soma (apical dendrites, respectively), and an axon that usually forms several local collaterals before leaving the neocortex to project to distant brain regions. Basal dendrites are localized around the soma while apical dendrites typically extend towards the pia, forming multiple oblique dendrites en route and terminating in a distinct tuft that is associated with high branching density. Apical dendrites impart unique functional properties to PCs and form the basis for the generation of active dendritic (Cuntz et al. 2007, van Elburg & van Ooyen 2010, Cuntz 2012, van Ooyen & van Elburg 2014, Bird & Cuntz 2016) and synaptic events, such as back-propagating action potentials (Stuart & Sakmann, 1994), calcium transients in dendrites (Markram & Sakmann, 1994; Schiller et al. 1995; Yuste et al. 2000), integration of synaptic inputs from different cortical layers (Larkum et al. 1999; Larkum et al. 2001; Schaefer et al. 2003; Spruston, 2008), and spike-timing dependent plasticity (Markram et al. 1997a; Sjöström et al. 2001; Froemke et al. 2005). The unique functional properties of apical dendrites are therefore essential for integrating top-down (from association areas) and bottom-up streams of input (from primary sensory and motor areas) to the neocortex to shape the output firing pattern of PCs. The characteristic morphological shapes of apical dendrites are associated with their unique functional properties, as objectively defined types of PCs also express unique firing patterns (Deitcher et al. 2017) and form distinct synaptic sub-networks within and across layers (Yoshimura et al. 2005; Kampa et al. 2006). Therefore, the branching properties of the apical trees are commonly used for their separation into morphological cell types (Ascoli & Krichmar 2000, Oberlaender et al. 2011, Marx and Feldmeyer 2012, Narayanan et al. 2017). The expert classification, which is based on visual inspection of the cells, usually makes it possible to distinguish the different shapes of morphologies and to group neurons into cell types. However, despite the expertise involved, visual inspection is subjective and often results in bioRxiv preprint doi: https://doi.org/10.1101/349977; this version posted June 19, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. non-consensual and ambiguous classifications (DeFelipe et al. 2013, Ledergerber and Larkum 2010, Marx and Feldmeyer 2012, Markram et al. 2015). A striking indication of this problem, as described previously (DeFelipe et al. 2013), is the fact that experts assign a different cell type to a neuron from the one they had chosen in their original study for the same neuron, independently of the reconstruction quality (DeFelipe et al. 2013). For this reason, an objective classification scheme is essential for a consensual and consistent definition of neuronal types, which can be achieved either by an objective supervised or unsupervised classification scheme. The objective supervised classification starts from the expert classification and verifies or disproves a proposed grouping based on objective measurements. When the expert classification cannot be supported by objective measurements, an objective unsupervised classification scheme is required. In this case, the classifier starts from a random classification and reassigns labels to the cells based on objective measurements until the classifier converges to a stable grouping proposal. To perform objective classification, the neuronal morphologies must be encoded in a digital format. The 3D digital reconstruction of a neuron encodes the path (in XYZ co-ordinates) and the thickness of each branch within its morphology and enables the consistent morphological analysis of its structure. The standard morphometrics (such as section length, bifurcation angles, etc.; Petilla Interneuron Nomenclature Group 2008, Ascoli & Krichmar 2000) that are commonly used as input measurements for objective classification, focus on different local aspects of the neuronal morphology and therefore must be used in combination with other morphological measurements. To avoid over-fitting, i.e., confusing the random noise in the biological structure with a significant discrimination factor, which is a result of using a large number of features in a few individual cells, feature selection is required. Appropriate feature selection is important for identifying the features that are indicative of the differences between neuronal shapes and that can be generalized across different brain regions and species. However, feature selection is often subjective, and the feature sets proposed by different experts are often inconsistent (DeFelipe et al. 2013). In addition, alternative sets of morphometrics result in different classifications (Kanari et al. 2017). To avoid this issue, a number of mathematically rigorous methods have been proposed for the morphological analysis of neurons (Van Pelt et al. 1991, DeFelipe et al. 2013, Gillette and Ascoli 2015a, Gillette et al. 2015B, Wan et al. 2015). We have developed an alternative representation of morphologies based on persistent homology (Carlsson, 2009) that provides a standardized quantification of neuronal branching structure (Kanari et al. 2017). bioRxiv preprint doi: https://doi.org/10.1101/349977; this version posted June 19, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. The Topological Morphology Descriptor (TMD) algorithm generates a barcode from a neuronal tree, coupling the topology of the branching structure with its geometry, and therefore encoding the overall shape of the tree in a single descriptor (Kanari et al. 2017). The TMD is a simplified representation of the original tree that retains key information to perform well in a discrimination task, by mapping the tree to a topological representation with less information loss than the usual morphometrics. The cell types proposed based on the TMD-classification are unbiased, since they are based on a mathematical descriptor of the tree's branching structure rather that the visual inspection of the cells, and thus this method is less prone to user-induced biases. There is no need to analyze
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